List of variants in gene CLN6 reported as benign for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017882.3(CLN6):c.486+8C>T	rs149692285	0.01339
NM_017882.3(CLN6):c.34G>A (p.Ala12Thr)	rs112239768	0.01081
NM_017882.3(CLN6):c.298-6C>T	rs117038427	0.00549
NM_017882.3(CLN6):c.769A>G (p.Ser257Gly)	rs151295143	0.00475
NM_017882.3(CLN6):c.339G>A (p.Thr113=)	rs146135801	0.00141
NM_017882.3(CLN6):c.214G>C (p.Glu72Gln)	rs104894483	0.00140
NM_017882.3(CLN6):c.270C>T (p.Asn90=)	rs145247814	0.00104
NM_017882.3(CLN6):c.487-15C>T	rs200775021	0.00049
NM_017882.3(CLN6):c.822G>A (p.Ala274=)	rs151186473	0.00041
NM_017882.3(CLN6):c.84-18C>T	rs201554701	0.00022
NM_017882.3(CLN6):c.282C>A (p.Pro94=)	rs139261571	0.00021
NM_017882.3(CLN6):c.585C>T (p.Gly195=)	rs144507672	0.00011
NM_017882.3(CLN6):c.63C>T (p.Gly21=)	rs796052348	0.00001
NM_017882.3(CLN6):c.135C>T (p.Leu45=)	rs374577694
NM_017882.3(CLN6):c.213C>G (p.Leu71=)	rs146980624
NM_017882.3(CLN6):c.297+19del	rs61224699
NM_017882.3(CLN6):c.64G>T (p.Ala22Ser)	rs527373013
NM_017882.3(CLN6):c.66C>T (p.Ala22=)	rs796052349
NM_017882.3(CLN6):c.83+14dup	rs756808642

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.